Some Gammaproteobacteria are enriched within CD14+ macrophages from intestinal lamina propria of Crohn's disease patients versus mucus

Sci Rep. 2020 Feb 19;10(1):2988. doi: 10.1038/s41598-020-59937-w.

Abstract

Crohn's disease causes chronic inflammation in the gastrointestinal tract and its pathogenesis remains unclear. In the intestine of Crohn's disease patients, CD14+CD11+CD163low macrophages contribute to inflammation through the induction of Th17 cells and production of inflammatory cytokines; the CD14+CD11c+163high fraction is anti-inflammatory through the production of IL-10 in normal cases. In this report, the 16S rRNA gene amplicon sequencing method was used to identify bacteria that are specifically present in intestinal CD14+CD11c+ macrophages of Crohn's disease patients. Bacteria present in intestinal CD14+CD11c+ macrophages and mucus of Crohn's disease patients were separated into different clusters in principal coordinates analysis. There was a statistically significant increase in the relative composition of CD14+CD11c+ macrophages from mucus in two phyla (Proteobacteria [p = 0.01] and Actinobacteria [p = 0.02]) and two families (Moraxellaceae [p < 0.001] and Pseudomonadaceae [p = 0.01]). In addition, OTU-1: Acinetobacter and OTU-8: Pseudomonadaceae tended to concentrate in the CD14+CD11c+CD163low subset, whereas OTU-10: Proteus, OTU-15: Collinsella tended to concentrate more in the CD14+CD11c+CD163high subset than the other subset and mucus.

Publication types

  • Observational Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Crohn Disease / immunology
  • Crohn Disease / microbiology*
  • Crohn Disease / pathology
  • Crohn Disease / surgery
  • DNA, Bacterial / isolation & purification
  • Female
  • Gammaproteobacteria / genetics
  • Gammaproteobacteria / immunology
  • Gammaproteobacteria / isolation & purification*
  • Humans
  • Ileum / cytology
  • Ileum / immunology
  • Ileum / microbiology*
  • Ileum / pathology
  • Intestinal Mucosa / cytology
  • Intestinal Mucosa / immunology
  • Intestinal Mucosa / microbiology*
  • Intestinal Mucosa / pathology
  • Lipopolysaccharide Receptors / metabolism
  • Macrophages / immunology
  • Macrophages / metabolism
  • Macrophages / microbiology*
  • Male
  • Middle Aged
  • RNA, Ribosomal, 16S / genetics
  • Young Adult

Substances

  • CD14 protein, human
  • DNA, Bacterial
  • Lipopolysaccharide Receptors
  • RNA, Ribosomal, 16S